Mechanical loading stimulates the release of transforming growth factor‐β activity by cultured mouse calvariae and periosteal cells
- 1 April 1995
- journal article
- research article
- Published by Wiley in Journal of Cellular Physiology
- Vol. 163 (1) , 115-119
- https://doi.org/10.1002/jcp.1041630113
Abstract
We have shown earlier that mechanical stimulation by intermittent hydrostatic compression (IHC) inhibits bone resorption and stimulates bone formation in cultured fetal mouse calvariae (Klein-Nulend et al., 1986, Arthritis Rheum., 29:1002–1009). The production of soluble bone factors by such calvariae is also modified (Klein-Nulend et al., 1993, Cell Tissue Res., 271:513–517). Transforming growth factor-β (TGF-β) is an important local regulator of bone metabolism and is produced by osteoblasts. In this study, the release of TGF-β activity as a result of mechanical stress was examined in organ cultures of neonatal mouse calvariae, in primary cultures of calvariae-derived osteoprogenitor (OPR) cells, and in more differentiated osteoblastic (OB) cells. Whole calvariae and calvariaederived cells were cultured in the presence or absence of IHC for 1–7 days and medium concentrations of active as well as total TGF-β were measured using a bioassay. IHC (maximum 13 kPa, maximal pressure rate 32.5 kPa/sec) was generated by intermittently (0.3 Hz) compressing the gas phase above the cultures. We found that mechanical loading by IHC stimulated the release of TGF-β activity from cultured calvariae by twofold after 1 day. IHC also stimulated the release of TGF-β activity from calvariae-derived cells after 1 and 3 days. The absolute amounts of TGF-β activity released were lower in OPR cells than in OB cells, but the stimulatory effect of IHC was greater in OPR cells. Total TGF-β (active and bound) released into the medium was not affected by IHC. IHC did not change the dry weight of the organ cultures, nor the DNA or protein content of the cell cultures. These data show that mechanical perturbation of bone cells, particularly OPR cells, enhances the activation of released TGF-β. We conclude that modulation of TGF-β metabolism may be part of the response of bone tissue to mechanical stress.Keywords
This publication has 26 references indexed in Scilit:
- THE ‘LAW OF BONE TRANSFORMATION’: A CASE OF CRYING WOLFF?Biological Reviews, 1991
- Inhibiting and stimulating effects of TGF-β1 on osteoclastic bone resorption in fetal mouse bone organ culturesJournal of Bone and Mineral Research, 1991
- In vivo effects of human recombinant transforming growth factor β on bone turnover in normal miceJournal of Bone and Mineral Research, 1990
- Cellular responses to mechanical loading in vitroJournal of Bone and Mineral Research, 1990
- Transforming growth factor-beta and the initiation of chondrogenesis and osteogenesis in the rat femur.The Journal of cell biology, 1990
- Inhibition of osteoclastic bone resorption by mechanical stimulation in vitroArthritis & Rheumatism, 1990
- Role of Transforming Growth Factor-Beta in Bone RemodelingClinical Orthopaedics and Related Research, 1990
- Osteopenia in the immobilized rat hind limb is associated with increased bone resorption and decreased bone formationBone, 1989
- Increased calcification of growth plate cartilage as a result of compressive force in vitroArthritis & Rheumatism, 1986
- β-Transforming Growth Factor is stored in human blood platelets as a latent high molecular weight complexBiochemical and Biophysical Research Communications, 1986